EP0663950B1 - Variantes de cellulase - Google Patents

Variantes de cellulase Download PDF

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Publication number
EP0663950B1
EP0663950B1 EP93922899A EP93922899A EP0663950B1 EP 0663950 B1 EP0663950 B1 EP 0663950B1 EP 93922899 A EP93922899 A EP 93922899A EP 93922899 A EP93922899 A EP 93922899A EP 0663950 B1 EP0663950 B1 EP 0663950B1
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EP
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Prior art keywords
endoglucanase
cellulase
enzyme
variant
detergent
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EP93922899A
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German (de)
English (en)
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EP0663950A1 (fr
Inventor
Martin Schülein
Henrik Fredholm
Carsten Mailand Hjort
Grethe Rasmussen
Egon Nielsen
Peter Rosholm
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Novozymes AS
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Novozymes AS
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Priority claimed from DK122392A external-priority patent/DK122392D0/da
Priority claimed from DK122592A external-priority patent/DK122592D0/da
Priority claimed from DK122492A external-priority patent/DK122492D0/da
Priority claimed from DK122192A external-priority patent/DK122192D0/da
Priority claimed from DK122292A external-priority patent/DK122292D0/da
Priority claimed from DK154392A external-priority patent/DK154392D0/da
Priority to EP04006060A priority Critical patent/EP1431389A3/fr
Application filed by Novozymes AS filed Critical Novozymes AS
Publication of EP0663950A1 publication Critical patent/EP0663950A1/fr
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/24—Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402—Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • C12N9/2405—Glucanases
    • C12N9/2434—Glucanases acting on beta-1,4-glucosidic bonds
    • C12N9/2437—Cellulases (3.2.1.4; 3.2.1.74; 3.2.1.91; 3.2.1.150)
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/38—Products with no well-defined composition, e.g. natural products
    • C11D3/386—Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38645—Preparations containing enzymes, e.g. protease or amylase containing cellulase
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y302/00—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
    • C12Y302/01—Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
    • C12Y302/01004—Cellulase (3.2.1.4), i.e. endo-1,4-beta-glucanase
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
    • D06M16/003—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic with enzymes or microorganisms
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
    • D06P5/02—After-treatment
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
    • D06P5/15—Locally discharging the dyes
    • D06P5/158—Locally discharging the dyes with other compounds
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
    • D06P5/13—Fugitive dyeing or stripping dyes
    • D06P5/137—Fugitive dyeing or stripping dyes with other compounds

Definitions

  • the present invention relates to endoglucanase variants with reduced sensitivity to oxidation.
  • Enzymes which are able to degrade cellulose may be used in paper pulp processing for removing the non-crystal-line parts of cellulose, thus increasing the proportion of crystalline cellulose in the pulp, and in animal feed for improving the digestibility of glucans.
  • a further important use of cellulolytic enzymes is for textile treatment, e.g.
  • the present invention relates to insert claim 1.
  • endoglucanase variants of the invention when used in detergent compositions, have improved properties as regards, reduced sensitivity to oxidation or the presence of a peroxidase bleaching system.
  • the invention also relates to detergent compositions comprising an endoglucanase variant of the invention.
  • V221S a deletion of valine in the same position is shown as: V221* and insertion of an additional amino acid residue such as threonine is shown as: V221ST
  • V221S + N222S + Q223T Multiple mutations are separated by pluses, i.e.: V221S + N222S + Q223T representing mutations in positions 221, 222 and 223 substituting serine and threonine for valine, asparagine and glutamine, respectively.
  • cellulose binding domain in the following abbreviated to CBD
  • CBD cellulose binding domain
  • an amino acid sequence e.g. as described in Kraulis, P., Clore, G.M., Nilges, M., Jones, T.A., Pettersson, G., Knowles, J. and Gronenborn, A.M. Determination of the three-dimensional structure of the C terminal domain of cellobiohydrolase I from Trichoderma reesei. A study using nuclear magnetic resonance and hybrid distance geometry-dynamical simulated annealing.. Biochemistry 28:7241-7257, 1989) capable of effecting binding of the cellulase variant to a cellulosic substrate.
  • catalytically active domain in the following abbreviated to CAD is intended to indicate the core region of the enzyme containing the catalytic site of the enzyme, vide e.g. Gideon et al.: Nature (1993) 365, p.362-364 .
  • linking region is intended to indicate a region adjoining the CBD and connecting it to the CAD of the enzyme.
  • the linking regions identified so far are characterized by being predominantly hydrophillic and uncharged, and by being enriched in certain amino acids to form short, repetitive units imparting flexibility to the sequence.
  • the flexible structure of the linking region is believed to facilitate the action of the catalytically active domain of the enzyme bound to a cellulosic substrate by the CBD. Examples of suitable linking regions are shown in N.R. Gilkes et al., Microbiol. Rev. 55 , 1991, pp. 303-315).
  • binding properties is intended to indicate the affinity with which the CBD binds to a cellulosic substrate, as well as the manner in which the CBD binds under different conditions. For instance the CBD may bind differently at different pH values. This behaviour under different conditions may be modified, e.g. by changing the electrostatic charge of the CBD as indicated above.
  • another CBD is intended to include a CBD derived from another cellulase; the additional CBD may be located at the N-terminal end of the catalytically active domain when the "native" CBD is located at the C-terminal end, and vice versa. Substitution by proline specifically is believed to influence the thermal and protease stability of the enzyme.
  • the parent endoglucanase is preferably a microbial endoglucanase.
  • the endoglucanase may be selected from bacterial endoglucanase, e.g. Pseudomonas endoglucanase or Bacillus , such as the Bacillus strains described in US 4,822,516, US 5,045,464 or EP 468 464, or B. lautus (cf. WO 91/10732), endoglucanase.
  • the parent cellulases may be a fungal cellulase, in particular Humicola , Trichoderma , Irpex, Aspergillus , Penicillium , Myceliophthora or Fusarium cellulases.
  • suitable parent cellulases are described in, e.g. WO 91/17244.
  • suitable Trichoderma cellulases are those described in T.T. Teeri, Gene 51 , 1987, pp. 43-52.
  • the parent cellulase is selected from the cellulases classified in family 45, e.g.
  • EG B Pseudomonas fluorescens
  • EG V Humicola insolens
  • a particularly preferred endoglucanase is one derived from a strain of Humicola insolens , such as a H . insolens endoglucanase, in particular a H . insolens 43 kD endoglucanase as described in WO 91/17243, or a homologue thereof.
  • the term "homologue” is intended to indicate a cellulase the amino acid sequence of which is at least 45% identical, over the full length, to the 43 kD endoglucanase or a cellulase that both adopts the same overall tertiary or three-dimensional (3D) fold as the 43 kD endoglucanase from H . insolens and has two acid residues that are involved in catalysis and placed in the active site cleft and optionally an additional acid residue being involved in catalysis and placed in the flexible loop facing the active site cleft.
  • Sequence comparisons may be performed via known algorithms, such as the one described by Lipman and Pearson, Science 227 , 1985, p. 1435.
  • the backbone of a protein can be divided into flexible and structurally conserved regions by means of structural analysis and sequential alignment of homologous proteins.
  • the flexible regions (FR) are the parts of the protein fold where the backbone conformation is likely to change during evolution.
  • the conserved regions (SCR) are the parts of the protein fold where the backbone conformation will be left largely unchanged, i.e. is expected o be conserved in other proteins having the same fold.
  • SCRs may specify known catalytic or other key residues.
  • a protein A is defined to have the same overall fold as a protein B if at least one of the following conditions are fulfilled:
  • homologues are the Pseudomonas fluorescens cellulase described by H.J. Gilbert et al., op . cit ., and the Fusarium oxysporum cellulase described in WO 91/17243, vide the attached Fig. 1 showing a sequence alignment of the three cellulases.
  • the term "elongated cleft” refers to a cleft which has dimensions permitting at least three glucose unit of ⁇ -1,4-glucan polymeric substrates access to the active site.
  • endoglucanase the catalytically active domain of which has the overall topology indicated above, i.e. the endoglucanase described in WO 91/17243 which in the following is referred to as EG V (endoglucanase V). It should, however, be understood that the present invention is in no way intended to be limited to variants of this particular endoglucanase.
  • Three crystal structures have been solved for EG V by X-ray crystallography.
  • the three structures describe the native enzyme (Gideon et al.: Nature (1993) 365, p.362-364 ), the native enzyme complexed with cellobiose (Gideon et al.: op . cit .) and the active site mutant D10N complexed with a product consisting of two cellotriose units (Gideon et al., personal communication).
  • the overall conformation of the enzyme is the same in all three structures with the exception of the flexible surface loop, which is invisible in the native structure, fixed in open position in the structure with cellobiose and in closed position in the structure with cellotriose products.
  • the cleft has a length of about 30 ⁇ , a width of about 9 ⁇ , and a depth of about 7 ⁇ .
  • the dimensions of the cleft are sufficient to permit binding of seven glucose units of ⁇ -1,4-glucans. These sites are labelled A, B, C, D, E, F, G, with cleavage occurring between site D and E.
  • Table 1 below is defined the atoms in EG V that interact with the glucose units at the different sites A-G. Analysis of the cleavage pattern of EG V has shown that binding to sites C-F is necessary for catalysis and that binding to the other sites enhance catalysis.
  • one of the products is bound to sites A-C and the other product is bound to sites E-G with site G being a weak binding site and not very well defined. It is possible to model in a glucose unit at site D with only a few steric overlaps. It is contemplated that the enzyme distorts the normal conformation of glucose unit at position D during catalysis.
  • the active site cleft is open at the surface to permit docking of a glucan polymer therein.
  • residue 111-119 changes conformation, with Leu115 moving about 13 ⁇ from a solvent exposed to a buried position, so as to enclose the glucan polymer in a tunnel at the cleavage point between site D and E.
  • the active site comprises two aspartic acids, Asp10 and Asp121.
  • EG V is an inverting enzyme with Asp10 functioning as the general base in the catalysis.
  • Asp114 and His119 has been found important for catalysis. Asp114 is involved in binding the glucose unit at site D and together with Ile131 it closes upon the glucose polymer and turns the cleft into a tunnel. It is contemplated that the purpose of the tunnel is to expel water from the environment around Asp121 and thereby stabilizing the protonated oxygen of Asp121. It has been found that His119 is involved in a hydrogen bond network through Thr6 to the other oxygen of Asp121. This hydrogen bond network may also help stabilizing the protonated form of Asp121.
  • the "channel" leading from the surface to the cleft (in this particular case there are two such channels) is believed to supply water to Asp10 for the hydrolysis of the glucan polymer.
  • the channel may by used as a means of expelling water from the said cleft during substrafe docking.
  • PI-interaction indicates interaction between two aromatic rings; “Through water” indicates cases where no water is present in the structure, but interaction with the substrate may take place through a water molecule; "Possible” indicates atoms that may interact with the substrate in other binding modes; “Steric” indicates no other apparent interaction than that; "Catalytic” indicates catalytic residue.
  • the additional CBD may for instance be derived from one of the cellulases described in WO 91/10732 or WO 91/17244 or Penttila, M.E., Lehtovaara, P., Nevalainen, H., Bhikhabhai, R. and Knowles, J. Homology between cellulase genes of Trichoderma reesei: complete nucleotide sequence of the endoglucanase I gene..
  • Regions I-X shown below correspond to the following positions in the 43 kD endoglucanase sequence: Region Residues I 2-21 II 44-48 III 55-60 IV 65-67 V 72-75 VI 95-103 VII 109-123 VIII 128-136 IX 142-148 X 175-185
  • one or more amino acid residues on the surface of the CAD are substituted by one or more amino acid residues which are less sensitive to oxidation or the presence of a peroxidase bleaching system;
  • the CAD comprising an elongated cleft containing the catalytically active site, at least one channel leading from the surface of the cellulase molecule to said cleft and supplying water to said cleft for the hydrolysis of cellulose at the active site, and a positively charged surface region in the vicinity of at least one amino acid residue of the active site.
  • tyrosine is sensitive to the presence of bleaching agents such as peroxidase systems, resulting in inactivation of the enzyme.
  • peroxidase system is intended to indicate a bleaching system comprising a peroxidase, a substrate for the peroxidase and a bleach accelerator, e.g. as described in WO 89/09813 or WO 91/05839. It has furthermore been found that this problem may be alleviated by appropriate substitutions by less sensitive amino acid residues, e.g. serine, asparagine, glutamine, proline, phenylalanine, glutamic acid, or glycine.
  • the surface conformation of the enzyme may be modified by substituting one or more tyrosine in position 8 and/or 147 or in a corresponding position in a homologue thereof.
  • amino acid residues are substituted as follows Y8F Y147F,H,S,Q,N,E,D.
  • the DNA sequence encoding a parent endoglucanase may be isolated from any cell or microorganism producing the cellulase in question by various methods, well known in the art. First a genomic DNA and/or cDNA library should be constructed using chromosomal DNA or messenger RNA from the organism that produces the endoglucanase to be studied. Then, if the amino acid sequence of the endoglucanase is known, homologous, labelled oligonucleotide probes may be synthesized and used to identify endoglucanase-encoding clones from a genomic library of bacterial DNA, or from a fungal cDNA library.
  • a labelled oligonucleotide probe containing sequences homologous to endoglucanase from another strain of bacteria or fungus could be used as a probe to identify endoglucanase-encoding clones, using hybridization and washing conditions of lower stringency.
  • Yet another method for identifying endoglucanase-producing clones would involve inserting fragments of genomic DNA into an expression vector, such as a plasmid, transforming endoglucanase-negative bacteria with the resulting genomic DNA library, and then plating the transformed bacteria onto agar containing a substrate for endoglucanase.
  • an expression vector such as a plasmid
  • transforming endoglucanase-negative bacteria with the resulting genomic DNA library
  • plating the transformed bacteria onto agar containing a substrate for endoglucanase Those bacteria containing endoglucanase-bearing plasmid will produce colonies surrounded by a halo of clear agar, due to digestion of the substrate by secreted cellulase.
  • the DNA sequence encoding the enzyme may be prepared synthetically by established standard methods, e.g. the phosphoamidite method described by S.L. Beaucage and M.H. Caruthers, Tetrahedron Letters 22 , 1981, pp. 1859-1869, or the method described by Matthes et al., The EMBO J. 3 , 1984, pp. 801-805.
  • phosphoamidite method oligonucleotides are synthesized, e.g. in an automatic DNA synthesizer, purified, annealed, ligated and cloned in appropriate vectors.
  • the DNA sequence may be of mixed genomic and synthetic, mixed synthetic and cDNA or mixed genomic and cDNA origin prepared by ligating fragments of synthetic, genomic or cDNA origin (as appropriate), the fragments corresponding to various parts of the entire DNA sequence, in accordance with standard techniques.
  • the DNA sequence may also be prepared by polymerase chain reaction (PCR) using specific primers, for instance as described in US 4,683,202 or R.K. Saiki et al., Science 239 , 1988, pp. 487-491.
  • mutations may be introduced using synthetic oligonucleotides. These oligonucleotides contain nucleotide sequences flanking the desired mutation sites; mutant nucleotides are inserted during oligonucleotide synthesis.
  • a single-stranded gap of DNA bridging the endoglucanase-encoding sequence, is created in a vector carrying the endoglucanase gene.
  • the synthetic nucleotide, bearing the desired mutation is annealed to a homologous portion of the single-stranded DNA.
  • a plasmid (pSX 320) enabling expression of the Humicola insolens -43kD endoglucanase (karyosome) in Aspergillus oryzae has been described in an earlier patent (PCT/DK 91/00123).
  • the gene encoding karyosome was subcloned from pSX 320 into pUC 19 (C. Yanisch-Perron et. al.(1985). Gene 33, 103-119) as described in figure 2.
  • a Cla I restriction site was introduced into pCaHj 170 in the 43 K gene as a silent site directed mutation in position 537. Site directed mutagenesis was done using the PCR method of Nelson and Long (R. M. Nelson, G. L.
  • the plasmids pCaHj 171 and pCaHj 201 was constructed from pCaHj 170 as shown in figure 4 and 5.
  • Two plasmids, pCaHj 416 and pCaHj 417, enabling the use of pCaHj 201 for mutant construction were made from the Aspergillus expression plasmid pHD 414 .
  • the construction of these plasmids are summarised in figure 6.
  • pCaHj 201 was used for construction of mutants as shown in figure 7.
  • the expression plasmids harbouring the mutated 43 K genes were transformed into Aspergillus oryzae IFO 4177 using selection on acetamide by cotransformation with pToC 90 as described in the patent application(PCT/DK/00123).
  • the mutant CC234, consisting of V221S, cN222S, Q223T was constructed using the oligonucleotide 4214.
  • the mutations were introduced as described in figure 6, subcloning the mutated Hind III - Sal I fragment into pCaHj 416.
  • the mutant CC248, consisting of A162P was constructed using the oligonucleotide 4271.
  • the mutation was introduced as described in figure 6, subcloning the mutated BamH I - Hind III fragment into pCaHj 417.
  • a mutated endoglucanase-coding sequence produced by methods described above, or any alternative methods known in the art can be expressed, in enzyme form, using an expression vector which typically includes control sequences encoding a promoter, operator, ribosome binding site, translation initiation signal, and, optionally, a repressor gene or various activator genes.
  • an expression vector typically includes control sequences encoding a promoter, operator, ribosome binding site, translation initiation signal, and, optionally, a repressor gene or various activator genes.
  • nucleotides encoding a "signal sequence" may be inserted prior to the cellulase-coding sequence.
  • a target gene to be treated according to the invention is operably linked to the control sequences in the proper reading frame.
  • Promoter sequences that can be incorporated into plasmid vectors, and which can support the transcription of the mutant cellulase gene include but are not limited to the prokaryotic ⁇ -lactamase promoter (Villa-Kamaroff, et al., 1978, Proc. Natl. Acad. Sci. U.S.A. 75 :3727-3731) and the tac promoter (DeBoer, et al., 1983, Proc. Natl. Acad. Sci. U.S.A. 80 :21-25). Further references can also be found in "Useful proteins from recombinant bacteria" in Scientific American, 1980, 242 :74-94.
  • B. subtilis is transformed by an expression vector carrying the mutated DNA. If expression is to take place in a secreting microorganism such as B . subtilis a signal sequence may follow the translation initiation signal and precede the DNA sequence of interest. The signal sequence acts to transport the expression product to the cell wall where it is cleaved from the product upon secretion.
  • control sequences as defined above is intended to include a signal sequence, when is present.
  • a filamentous fungus is used as the host organism.
  • the filamentous fungus host organism may conveniently be one which has previously been used as a host for producing recombinant proteins, e.g. a strain of Aspergillus sp., such as A. niger , A. nidulans or A. oryzae .
  • a strain of Aspergillus sp. such as A. niger , A. nidulans or A. oryzae .
  • the use of A. oryzae in the production of recombinant proteins is extensively described in, e.g. EP 238 023.
  • the DNA sequence coding for the endoglucanase variant is preceded by a promoter.
  • the promoter may be any DNA sequence exhibiting a strong transcriptional activity in Aspergillus and may be derived from a gene encoding an extracellular or intracellular protein such as an amylase, a glucoamylase, a protease, a lipase, a cellulase or a glycolytic enzyme.
  • suitable promoters are those derived from the gene encoding A. oryzae TAKA amylase, Rhizomucor miehei aspartic proteinase, A. niger neutral ⁇ -amylase, A. niger acid stable ⁇ -amylase, A. niger glucoamylase, Rhizomucor miehei lipase, A. oryzae alkaline protease or A. oryzae triose phosphate isomerase.
  • a preferred promoter for use in the process of the present invention is the A. oryzae TAKA amylase promoter as it exhibits a strong transcriptional activity in A. oryzae .
  • the sequence of the TAKA amylase promoter appears from EP 238 023.
  • Termination and polyadenylation sequences may suitably be derived from the same sources as the promoter.
  • the techniques used to transform a fungal host cell may suitably be as described in EP 238 023.
  • the DNA sequence encoding the cellulase variant may be preceded by a signal sequence which may be a naturally occurring signal sequence or a functional part thereof or a synthetic sequence providing secretion of the protein from the cell.
  • the signal sequence may be derived from a gene encoding an Aspergillus sp. amylase or glucoamylase, a gene encoding a Rhizomucor miehei lipase or protease, or a gene encoding a Humicola cellulase, xylanase or lipase.
  • the signal sequence is preferably derived from the gene encoding A. oryzae TAKA amylase, A. niger neutral ⁇ -amylase, A. niger acid-stable ⁇ -amylase or A. niger glucoamylase.
  • the medium used to culture the transformed host cells may be any conventional medium suitable for growing Aspergillus cells.
  • the transformants are usually stable and may be cultured in the absence of selection pressure. However, if the transformants are found to be unstable, a selection marker introduced into the cells may be used for selection.
  • the mature endoglucanase protein secreted from the host cells may conveniently be recovered from the culture medium by well-known procedures including separating the cells from the medium by centrifugation or filtration, and precipitating proteinaceous components of the medium by means of a salt such as ammonium sulphate, followed by chromatographic procedures such as ion exchange chromatography, affinity chromatography, or the like.
  • the endoglucanase variant may typically be added as a component of a detergent composition.
  • a detergent composition may be included in the detergent composition in the form of a non-dusting granulate, a liquid, in particular a stabilized liquid, or a protected enzyme.
  • Non-dusting granulates may be produced, e.g., as disclosed in US 4,106,991 and 4,661,452 (both to Novo Industri A/S) and may optionally be coated by methods known in the art.
  • Liquid enzyme preparations may, for instance, be stabilized by adding a polyol such as propylene glycol, a sugar or sugar alcohol, lactic acid or boric acid according to established methods. Other enzyme stabilizers are well known in the art.
  • Protected enzymes may be prepared according to the method disclosed in EP 238,216.
  • the detergent composition may further include one or more other enzymes, such as a protease, lipase, peroxidase, oxidase or amylase, conventionally included in detergent additives.
  • the detergent composition of the invention may be in any convenient form, e.g. as powder, granules or liquid.
  • a liquid detergent may be aqueous, typically containing up to 90% water and 0-20% organic solvent.
  • the detergent composition comprises a surfactant which may be anionic, non-ionic, cationic, amphoteric or a mixture of these types.
  • the detergent will usually contain 0-50% anionic surfactant such as linear alkyl benzene sulphonate (LAS), alpha-olefin sulphonate (AOS), alkyl sulphate (AS), alcohol ethoxy sulphate (AES) or soap.
  • LAS linear alkyl benzene sulphonate
  • AOS alpha-olefin sulphonate
  • AS alkyl sulphate
  • AES alcohol ethoxy sulphate
  • non-ionic surfactant such as nonyl phenol ethoxylate or alcohol ethoxylate.
  • it may contain a polyhydroxy fatty acid amide surfactant (e.g. as described in WO 92/06154).
  • the detergent composition may additionally comprise one or more other enzymes, such as an amylase, lipase, peroxidase, oxidase, esterase, cellulase, endoglucanase type II or protease.
  • enzymes such as an amylase, lipase, peroxidase, oxidase, esterase, cellulase, endoglucanase type II or protease.
  • the pH (measured in aqueous detergent solution) will usually be neutral or alkaline, e.g. 7-11.
  • the detergent may contain 1-40% of a detergent builder such as zeolite, phosphate, phosphonate, citrate, NTA, EDTA or DTPA, alkenyl succinic anhydride, or silicate, or it may be unbuilt (i.e. essentially free of a detergent builder). It may also contain other conventional detergent ingredients, e.g. fabric conditioners, foam boosters, bleaching agents, e.g.
  • TAED tetraacetyl ethylene diamine
  • NOBS nonanoyloxybenzene sulphonate
  • anti-corrosion agents soil-suspending agents
  • sequestering agents anti-soil redeposition agents
  • foam depressors dyes, bactericides, optical brighteners or perfumes.
  • the detergent compositions a)-h) include a endoglucanase variant of the invention and optionally one or more other enzymes, as indicated above.
  • the endoglucanase variant may be added in an amount corresponding to 0.001-100 mg enzyme per litre of wash liquor.
  • the S-CEVU assay quantifies the amount of catalytic activity present in the sample by measuring the ability of the sample to reduce the viscosity of a solution of carboxymethylcellulose (CMC). This activity is only related to the enzyme core and is unaffected by the presence or absence of the linking region and the CBD region.
  • the S-CEVU assay is carried out at 40°C, pH 7.5 using an relative enzyme standard for reducing the viscosity of the substrate (CMC).
  • the method is available from the Applicant as No. AF-302/2GB upon request.
  • the Dyed Avicel Assay quantifies the amount of cellulase able to attach to insoluble cellulose and release dye bound to the surface of the cellulosic powder.
  • Cellulases without the linking region and the CBD region exhibit low activity on this substrate and the assay can therefore be used to monitor the proteolytic degradation of intact endoglucanase to enzyme core.
  • the DAA correlates to some degree with the washing performance of endoglucanase stored in detergent containing protease enzyme(s).
  • pH of the Sigmacell/dye solution was adjusted to 11.5 by adding about 150 ml of the trisodium phosphate solution.
  • the mixture was stirred for 60 minutes at 55°C.
  • the mixture was vacuum filtered by means of a 1000 ml Büchner funnel and Whatman No.54 filter paper.
  • the filter cake was washed repeatedly with deionized water at 70°C - 80°C until the optical density at 590 nm (OD 590 ) of the filtrate (the waste water) was below 0.03.
  • the filter cake was rinsed with 100 ml of 50% ethanol resulting in further removal of blue colour and subsequent with 100 ml of 96% ethanol.
  • the cellulose was removed from the funnel and left to dry (in clean bench).
  • Tri-Sodium Phosphate (Merck 6578) 19 g Deionised water add 950 ml Berol 160 20 g Stir until completely clear. Deionised water fill up to 1000 ml
  • Samples are diluted in 0.1M phosphate buffer to a concentration of eg. 4, 8, 12, 16 S-CEVU/ml
  • Variomag Telesystem HP 60 P submersible magnetic stirrer plate, (60 points).
  • Variomag Test Tube Rack HP 60 for 16 mm test tubes. Test tubes, 16 mm ⁇ Magnetic stirring rods, 3x8 mm. Filter paper ⁇ 9 cm, Munktell 1F. Filtrating funnels Finnpipette 1-5ml Test tubes and rack for collection of the filtrate Magnetic stirrer plate and magnet for substrate suspension.
  • the temperature of the water bath must be 40°C. 2 ml of sample or standard solution were measured into test tubes placed in rack. When all tubes were ready, rack was placed in the water bath. A magnetic stirring rod was added to all tubes, the stirrer plate was started at 600 rpm. With 10 seconds interval, 2 ml of Dyed Cellulose Substrate was added with constant stirring during the pipetting. After 60 min reaction time 2 ml Nonionic stop reagent was added to each tube. The well mixed sample at 40°C was poured onto a paper filter in a filtrating funnel, and the clear filtrate was collected. The filtration must be repeated, if the filtrate is unclear. The absorbance at 590 nm of the filtrate was measured.
  • the dose-response curve is not linear, (Fig. 8), and the activity of the sample relative to the standard, (or of a stored sample relative to a non-stored sample) can be calculated as shown.
  • Fig. 9 shows an example of curves from Dyed Avicel Assay with endoglucanase variant I.
  • the test adsorbent was stored as suspension in distilled water, the content of dry cellulose (typically 15 g/l) being determined by drying and weighting an aliquot in a separate experiment.
  • the adsorbent was dosed by volume (0 - 0.5 ml) into plastic tubes, that can be sealed, to receive content of cellulose dry mass in the range of 0 - 8 mg. The volume was adjusted to 0.5 ml by distilled water.
  • Ariel Color which is a commercial compact powder detergent was pretreated in order to inactivate enzymes present in the powder detergent by incubating the detergent in a microwave oven for 8 min. at 85°C.
  • the suspension was shaken for 60 min on a Swelab Instrument 440 mixer at 20°, 1 sec -1 and the substrate with enzyme adsorbed was sedimented by centrifuging at 2500 g , 20° for 5 min.
  • the supernatant was assayed for the unbound endoglucanase activity using a conventional technique such as Red CMC assay (Tikhomirov D.F. et al., Biotechnologia (Moscow), translated into English by Plenum Press, 1989, Vol. 5, No. 4, p. 518-524).
  • Enzyme aliquots of 100 ⁇ l were added to 1 ml of 1% Red CMC substrate ( Fermentas Co., Vilnius, Lithuania), pH 7.5 (0.05 M Tris buffer), in narrow glass tubes, the mixture being transferred to a water thermostat, 40°, for 40 min. One more tube was added to the thermostat with buffer instead of enzyme aliquot as blank. The enzymatic reaction was stopped by addition of 1 ml of 80% ethanol containing 0.1 M CaCl 2 with subsequent vigorous shaking. The unhydrolysed substrate was separated by centrifuging the same tubes at 4000 g for 10 min and the supernatant absorbance at 490 nm was measured against water.
  • Red CMC substrate Fermentas Co., Vilnius, Lithuania
  • pH 7.5 0.05 M Tris buffer
  • the degree of adsorption was plotted in terms of the A 0 /A super ratio versus the adsorbent concentration - a linearisation method which gives a straight line in case of a single endoglucanase isoform, homogeneous according to adsorption properties (Klyosov A.A. et al ., Bioorgan . Chem. (Moscow), translated into English by Plenum Press, 1982, Vol. 8, No. 5, p. 643-651).
  • the constant of distribution, K d A bound /(A super . [S]), may be determined from this plot as the slope of the line.
  • the peroxidase system (POD system) used for Dye Transfer Inhibition (DTI), comprising a Coprinus cinereus peroxidase (CiP, obtained according to EP Patent Application 179,486), hydrogen peroxide, and p-hydroxy benzene sulphonate (pHBS) as peroxidase enhancing agent was simulated in a Britton-Robinson buffer, pH 8.5:
  • the 43 kD cellulase and the cellulase variant Y147S were incubated with the POD system for 10 min at 35 °C. Samples were withdrawn and diluted 5 times with ice-cold 0.1 M sodium phosphate, pH 7.0. The residual activities of the cellulases were measured by the CMCU method using the ferricyanide detection principle.
  • Substrate preparation 20 gram acid-swollen AVICEL • stock solution (see below for a preparation which can be stored for one month) was centrifuged for 20 min. at 5000 rpm., the supernatant was poured off, and the sediment was resuspended in 30 ml of buffer. Then centrifuged for 20 min. at 5000 rpm, the supernatant was poured off, and the sediment was resuspended in buffer to a total of 30 g.. This corresponds to a substrate concentration of 10 g AVICEL/litre. Buffer: 0.1M Barbital at pH 8.5 or 0.1M Glycine at pH 10.0
  • the enzymes were diluted to an activity of 0.5 S-CEVU/ml at pH 8.5 or 0.75 S-CEVU/ml at pH 10.0.
  • the substrate/buffer solution was preheated for 5 min at 40 °C. Then the enzyme solution was added and the solution was whirlmixed for 5 sec., followed by incubation for 20 min. at 40 °C. The reaction was stopped by adding 500 ⁇ l 2% NaOH solution, followed by whirlmixing for 5 sec. The samples were centrifuged for 20 min. at 5000 rpm. 1000 ⁇ l of supernatant was transferred from the test tubes to new test tubes, and 500 ⁇ l PHBAH-reagent was added, followed by boiling for 10 min. The test tubes were cooled in ice water. The absorbance of the samples were measured on a spectrophotometer at 410 nm.
  • a stock solution containing 300 mg/l was diluted to 5, 10, 15 and 25 mg/l. 1000 ⁇ l of the diluted standards were mixed with 500 ⁇ l of PHBAH-reagent, and were treated as the other samples, see above.
  • the release of reducing glucose equivalent was calculated using the standard curve.
  • the enzyme concentration was calculated using the molar absorbance of 61300 ( ⁇ ) for the 43 kD endoglucanase.
  • the K m , V max and K cat was calculated from a Lineweaver-Burk plot using different substrate concentrations.
  • the molar absorbance of the cellulase variants having substituted tyrosines and tryptophanes was adjusted accordingly using a absorbance value for tryptophane of 5690( ⁇ ) and for tyrosine of 1280( ⁇ ) and cystein 120( ⁇ ).
  • ⁇ The extinction coefficients ( ⁇ ) are disclosed in Gill,S.C. and Hippel, P.H.: Calculation of protein extinction coefficients from amino acid sequence data; Analytical Biochemistry vol 182, (319-326),(1989).
  • Each of the tested cellulase variants was purified to high homogeneity giving a single band in SDS-PAGE analysis (the ratio A 280 /A 260 was checked as being above 1.5).
  • the Acetone and the phosphoric-acid was cooled on ice.
  • the 5 g. Avicel • was moistened with water, then 150 ml of ice cold 85% Ortho-phosphoric-acid was added, and the mixture was placed on ice bath with weak stirring for 1 h.
  • 100 ml of ice cold acetone was added with stirring, followed by transfer of the mixture to a glass filter funnel, followed by washing with 3 x 100 ml ice cold acetone and dry suction after each washing.
  • the filter cake was washed with 2 x 500 ml water and sucked as dry as possible after each wash.
  • the filter cake was resuspended to a total volume of 300 ml and blended to homogeneity (using the Ultra Turrax Homogenizer).
  • the resulting product was stored in a refrigerator.
  • the cellulase was incubated with different concentrations of LAS (linear alkyl benzene sulphonate; Nansa 1169/P) for 10 min at 40°C.
  • LAS linear alkyl benzene sulphonate
  • LAS was diluted in 0.1 M phosphate buffer pH 7.5. The following concentrations were used: 500 ppm, 250 ppm, 100 ppm, 50ppm, 25ppm, and 10 ppm on no LAS.
  • the endoglucanase was diluted in the different LAS buffers to 0,2 S-CEVU/ml final concentration in a total volume of 10 ml and incubated for 10 min in a temperature controlled water bath.
  • the two samples of 0,5 ml solution were mixed with 1,5 ml 1% CMC solution (Hercules 7L) prepared in the same phosphate buffer, incubation for 20 min at 40°C, and then stopped with PHBAH, sodium tartrate in 2% NaOH.
  • the samples was cooked for 10 min and the absorbance was measured at 410 nm.
  • the activity was measured after subtraction of the blank.
  • the activity with no LAS was 100%.

Claims (8)

  1. Variant d'endoglucanase d'une endoglucanase bactérienne de base, où ladite endoglucanase de base est l'endoglucanase de 43 kDa provenant de Humicola insolens, présentée sur la Figure 1 sous le nom 43kdhum, ou une endoglucanase dont la séquence d'acides aminés présente une identité d'au moins 45 %, en pleine longueur, avec ladite endoglucanase de 43 kDa provenant de Humicola insolens, où une ou plusieurs tyrosines, sur une position correspondant aux positions 8 et 147 de l'endoglucanase de base de 43 kDa provenant de Humicola insolens, sont remplacées par une sérine, une asparagine, une glutamine, une proline, une phénylalanine, un acide glutamique, une arginine ou une glycine.
  2. Variant d'endoglucanase selon la revendication 1, dans lequel ledit remplacement est choisi dans l'ensemble comprenant Y8F et Y147F,H,S,Q,N,E,D.
  3. Variant d'endoglucanase selon la revendication 1, dans lequel l'endoglucanase de base est une endoglucanase fongique.
  4. Variant d'endoglucanase selon la revendication 3, dans lequel l'endoglucanase de base dérive d'une souche de Humicola, Trichoderma, Myceliophthora, Penicillium, Irpex, Aspergillus ou Fusarium.
  5. Variant d'endoglucanase selon la revendication 4, dans lequel l'endoglucanase de base est une endoglucanase de Humicola insolens, de préférence une endoglucanase de 43 kD de Humicola insolens.
  6. Composition détergente, comprenant un variant d'endoglucanase selon l'une quelconque des revendications précédentes, et un tensioactif.
  7. Composition détergente selon la revendication 6, qui comprend en outre une ou plusieurs enzymes choisies dans l'ensemble comprenant les protéases, les lipases, les peroxydases, les estérases, les cellulases, les endoglucanases de type II, les oxydases et les amylases.
  8. Composition détergente selon la revendication 7, où la composition détergente est une poudre ou une composition liquide.
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ATE262035T1 (de) 2004-04-15
DE69333454T2 (de) 2005-01-20
US6114296A (en) 2000-09-05
MX9306229A (es) 1994-05-31
WO1994007998A1 (fr) 1994-04-14
KR100303622B1 (ko) 2001-09-24
EP1431389A3 (fr) 2004-06-30
KR100303621B1 (ko) 2001-09-24
EP1431389A2 (fr) 2004-06-23
FI951629A (fi) 1995-04-05
FI951629A0 (fi) 1995-04-05
US5792641A (en) 1998-08-11

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